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BioWorld - Monday, July 27, 2026
Home » Topics » Disease categories and therapies » Ocular

Ocular
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STK-002 enters preclinical toxicology studies for autosomal dominant optic atrophy

March 11, 2022

Akebia Therapeutics reports prolyl 4-hydroxylase inhibitors

March 8, 2022
Cancer cell destruction by nanoparticles

Engineered retinal cells stare daggers at peritoneal tumors

March 4, 2022
By Anette Breindl
By using engineered retinal pigment epithelial cells to deliver IL-2 into the tumor microenvironment, investigators at Rice University eradicated ovarian and colorectal tumors in mouse models, and elicited T-cell responses after implantation in primates.
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Type II interferon restricts severity of NMO in a new preclinical model

Feb. 28, 2022
Rafiq Hasan, CEO, Complement Therapeutics
Newco news

Complement Therapeutics emerges from stealth with plan to take on untreatable eye disease

Feb. 23, 2022
By Richard Staines
U.K. biotech Complement Therapeutics Ltd has come out of stealth mode with €5 million ($5.7 million) in seed funding to tackle complement-related diseases, initially targeting the currently untreatable condition geographic atrophy due to dry age-related macular degeneration.
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Face with digital focus on eye
Newco news

Anti-VEGF pioneers pursue next-gen ocular therapies with Eyebio

Feb. 23, 2022
By Nuala Moran
LONDON – The team that opened up the market for anti-vascular endothelial growth factor (VEGF) drugs in the treatment of eye diseases has formed a new company, Eyebio Ltd., with the aim of developing a new generation of ocular therapies. David Guyer and Anthony Adamis, founders of Eyetech Pharmaceuticals Inc., which brought Macugen (pegaptanib sodium) through to FDA approval in December 2004, set up Eyebio in August last year, with seed funding from SV Health Investors.
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Kodiak moment spoiled, shares bearish as AMD study fails to Dazzle

Feb. 23, 2022
By Randy Osborne
Kodiak Sciences Inc. shares (NASDAQ:KOD) closed at $9.86, down $40.49, or 80.42% after the firm unveiled top-line data from its randomized, double-masked, active comparator-controlled phase IIb/III trial testing KSI-301, an antibody biopolymer conjugate, in treatment-naïve subjects with wet age-related macular degeneration (AMD).
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Pyruvate kinase isozyme M2 activators identified at the University of Michigan

Feb. 17, 2022

Splicebio raises record series A to tackle AAV packing problem

Feb. 16, 2022
By Nuala Moran
LONDON – In the largest-ever series A for a Spanish biotech, Splicebio S.L. has raised €50 million (US$56.9 million) to apply its protein splicing technology to the delivery of large genes that do not fit into existing vectors. The company claims its approach will overcome the capacity constraints of adeno-associated viral vectors (AAVs), by splitting genes into parcels and reconstituting the proteins they express in vivo.
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Optogenetics illustration

Proqr stock staggers as phase II/III study in rare genetic disease misses

Feb. 11, 2022
By Lee Landenberger
Proqr Therapeutics NV stock lost three-quarters of its value as word got out that its pivotal phase II/III study of sepofarsen in treating a tough, rare and genetic retinal disease failed to hit the primary endpoint. CEO Daniel de Boer said he was “shocked by the unexpected outcome” based on data from earlier studies. He added that he is unsure if Proqr will continue developing its therapy for treating CEP290-mediated Leber congenital amaurosis 10 until it understands the new results.
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